Novel loss-of-function mutation in BRCA2 gene identified in a Chinese female with a family history of ovarian cancer: A case report

Inherited loss-of-function mutations in the tumor suppressor BRCA2 gene are associated with a high risk of ovarian cancer in the Chinese population. The current case report discusses a novel heterozygous insertion in BRCA2 gene, c.3195_3196insA, in a 54-year-old Chinese female with hereditary ovaria...

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Detalles Bibliográficos
Autores principales: Cui, Yanzhi, Wang, Yanyan, Zhang, Ningzhi, He, Jun, Huang, Hui, Liu, Fengling, Wei, Suju, Dong, Qian, Wu, Jing, Lin, Keke, Chen, Weixi, Xiang, Jiale, Jin, Hui, Peng, Zhiyu, Zhao, Qiang, Li, Wei, Jiang, Da, Banerjee, Santasree
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396105/
https://www.ncbi.nlm.nih.gov/pubmed/30867769
http://dx.doi.org/10.3892/ol.2019.9950

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396105/
https://www.ncbi.nlm.nih.gov/pubmed/30867769
http://dx.doi.org/10.3892/ol.2019.9950

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